N/S/B-doped graphitized carbon encased Fe species as a highly active and durable catalyst towards oxygen reduction reaction

被引:29
作者
Li, Guang-Lan [1 ]
Cheng, Guang-Chun [1 ]
Chen, Wen-Wen [1 ]
Liu, Cai-Di [1 ]
Yuan, Li-Fang [1 ]
Yang, Bei-Bei [1 ]
Hao, Ce [1 ]
机构
[1] Dalian Univ Technol, State Key Lab Fine Chem, Panjin 124221, Liaoning, Peoples R China
关键词
N; S and B encased Fe; Carbon materials; Electrocatalyst; Oxygen reduction reaction; METAL-FREE ELECTROCATALYSTS; POROUS CARBON; EFFICIENT ELECTROCATALYST; NITROGEN; GRAPHENE; NANOTUBES; SULFUR; BORON; ALKALINE; PERFORMANCE;
D O I
10.1016/j.jcis.2017.12.012
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Exploring cost-effective, high-performance and durable non-precious metal catalysts is of great significance for the acceleration of sluggish oxygen reduction reaction (ORR). Here, we report an intriguing heteroatom-doped graphitized carbon encased Fe species composite by introducing N, S and B sequentially. The experimental approach was designed ingeniously for that the FeCl3 center dot 6H(2)O could catalyze thiourea to synthesize N, S co-doped carbon materials which would further react with H3BO3 and NH3 (emerged at the heat-treatment process) to prepare N, S and B co-doped carbon materials (Fe-N/S/B-C). The Fe-N/S/B-C exhibits an impressive ORR activity for its half-wave potential of -0.1 V, which is 36 mV or 19 mV higher than that of the corresponding single or dual doped counterparts (Fe-N-C or Fe-N/S-C) and 31 mV positive than that of Pt/C catalyst, respectively. Further chronoamperometric measurement and accelerated aging test confirm the excellent electrochemical durability of Fe-N/S/B-C with the stable core-shell structure. The remarkable ORR performance and facile preparation method enable Fe-N/S/B-C as a potential candidate in electrochemical energy devices. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:108 / 116
页数:9
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